CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

Large and rare copy number variants (CNVs) at several loci have been shown to increase risk for schizophrenia. Aiming to discover novel susceptibility CNV loci, we analyzed 6882 cases and 11 255 controls genotyped on Illumina arrays, most of which have not been used for this purpose before. We ident...

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Bibliografski detalji
Glavni autori: Rees, Elliott, Walters, James T.R., Chambert, Kimberly D., O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L., Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E., Moran, Jennifer L., Genovese, Giulio, Levinson, Douglas, Morris, Derek W., Cormican, Paul, Kendler, Kenneth S., O'Neill, Francis A., Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F., Gejman, Pablo V., McCarroll, Steven A., O'Donovan, Michael C., Owen, Michael J., Kirov, George
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2014
Teme:
Association Studies Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3929090/
https://ncbi.nlm.nih.gov/pubmed/24163246
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt540
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